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rs62508695

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62508695(A;A)
Make rs62508695(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102894875
GenePAH
is asnp
is mentioned by
dbSNPrs62508695
ebirs62508695
HLIrs62508695
Exacrs62508695
Varsomers62508695
Maprs62508695
PheGenIrs62508695
hapmaprs62508695
1000 genomesrs62508695
hgdprs62508695
ensemblrs62508695
gopubmedrs62508695
geneviewrs62508695
scholarrs62508695
googlers62508695
pharmgkbrs62508695
gwascentralrs62508695
openSNPrs62508695
23andMers62508695
23andMe allrs62508695
SNP Nexus

SNPshotrs62508695
SNPdbers62508695
MSV3drs62508695
GWAS Ctlgrs62508695
Max Magnitude0
ClinVar
Risk rs62508695(A;A)
Alt rs62508695(A;A)
Reference rs62508695(G;G)
Significance Untested
Disease not provided not specified
Variation info
Gene PAH
CLNDBN not provided not specified
Reversed 1
HGVS NC_000012.11:g.103288653C>T
CLNSRC
CLNACC RCV000088876.3, RCV000212762.1,